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Sara Wells

Showing results (91-100 of 154) with videos related to

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The Journal of Physiology|July 2, 2020
Age-related changes in the biophysical and morphological characteristics of mouse cochlear outer hair cellsJing-Yi Jeng, Stuart L Johnson, Adam J Carlton, et al.
Plos Genetics|October 27, 2011
HIF-VEGF pathways are critical for chronic otitis media in Junbo and Jeff mouse mutantsMichael T Cheeseman, Hayley E Tyrer, Debbie Williams, et al.
Plos Biology|October 9, 2019
Correction: Loss of Bardet-Biedl syndrome proteins causes synaptic aberrations in principal neuronsNaila Haq, Christoph Schmidt-Hieber, Fernando J Sialana, et al.
Plos Biology|September 4, 2019
Loss of Bardet-Biedl syndrome proteins causes synaptic aberrations in principal neuronsNaila Haq, Christoph Schmidt-Hieber, Fernando J Sialana, et al.
Plos Genetics|August 15, 2017
A mutation in Nischarin causes otitis media via LIMK1 and NF-κB pathwaysMichael Crompton, Tom Purnell, Hayley E Tyrer, et al.
Nucleic Acids Research|November 26, 2009
EuroPhenome: a repository for high-throughput mouse phenotyping dataHugh Morgan, Tim Beck, Andrew Blake, et al.
JCI Insight|February 15, 2017
G<b>α</b><sub>11</sub> mutation in mice causes hypocalcemia rectifiable by calcilytic therapyCaroline M Gorvin, Fadil M Hannan, Sarah A Howles, et al.
Endocrinology|June 3, 2017
Mutant Mice With Calcium-Sensing Receptor Activation Have Hyperglycemia That Is Rectified by Calcilytic TherapyValerie N Babinsky, Fadil M Hannan, Reshma D Ramracheya, et al.
Science Advances|August 28, 2020
Forward genetics identifies a novel sleep mutant with sleep state inertia and REM sleep deficitsGareth T Banks, Mathilde C C Guillaumin, Ines Heise, et al.
Biorxiv : the Preprint Server for Biology|November 24, 2025
International Mouse Phenotyping Consortium: Investigating gene function and providing insights into human diseaseRobert Wilson, Tuğba Bülbül Ataç, Tsz Kwan Cheng, et al.
Pageof 16

Showing results (91-100 of 154) with videos related to

Sort By:
Pageof 16
The Journal of Physiology|July 2, 2020
Age-related changes in the biophysical and morphological characteristics of mouse cochlear outer hair cellsJing-Yi Jeng, Stuart L Johnson, Adam J Carlton, et al.
Plos Genetics|October 27, 2011
HIF-VEGF pathways are critical for chronic otitis media in Junbo and Jeff mouse mutantsMichael T Cheeseman, Hayley E Tyrer, Debbie Williams, et al.
Plos Biology|October 9, 2019
Correction: Loss of Bardet-Biedl syndrome proteins causes synaptic aberrations in principal neuronsNaila Haq, Christoph Schmidt-Hieber, Fernando J Sialana, et al.
Plos Biology|September 4, 2019
Loss of Bardet-Biedl syndrome proteins causes synaptic aberrations in principal neuronsNaila Haq, Christoph Schmidt-Hieber, Fernando J Sialana, et al.
Plos Genetics|August 15, 2017
A mutation in Nischarin causes otitis media via LIMK1 and NF-κB pathwaysMichael Crompton, Tom Purnell, Hayley E Tyrer, et al.
Nucleic Acids Research|November 26, 2009
EuroPhenome: a repository for high-throughput mouse phenotyping dataHugh Morgan, Tim Beck, Andrew Blake, et al.
JCI Insight|February 15, 2017
G<b>α</b><sub>11</sub> mutation in mice causes hypocalcemia rectifiable by calcilytic therapyCaroline M Gorvin, Fadil M Hannan, Sarah A Howles, et al.
Endocrinology|June 3, 2017
Mutant Mice With Calcium-Sensing Receptor Activation Have Hyperglycemia That Is Rectified by Calcilytic TherapyValerie N Babinsky, Fadil M Hannan, Reshma D Ramracheya, et al.
Science Advances|August 28, 2020
Forward genetics identifies a novel sleep mutant with sleep state inertia and REM sleep deficitsGareth T Banks, Mathilde C C Guillaumin, Ines Heise, et al.
Biorxiv : the Preprint Server for Biology|November 24, 2025
International Mouse Phenotyping Consortium: Investigating gene function and providing insights into human diseaseRobert Wilson, Tuğba Bülbül Ataç, Tsz Kwan Cheng, et al.
Pageof 16